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PHARMA JOBS POST > Pharma Jobs > Emcure Pharmaceuticals Walk-in Drive on November 15 2025: Jobs at Gujarat OSD Plant
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Emcure Pharmaceuticals Walk-in Drive on November 15 2025: Jobs at Gujarat OSD Plant

Sunil Kumar Swain
Last updated: October 31, 2025 3:39 am
Sunil Kumar Swain 12 months ago
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Emcure Pharmaceuticals Announces Major Walk-in Drive for Gujarat OSD Plant

Surendranagar, Gujarat – In a significant recruitment initiative, Emcure Pharmaceuticals Ltd., a renowned name in the Indian pharmaceutical industry, has announced a comprehensive walk-in interview event. The drive aims to fill numerous positions across various departments at its state-of-the-art Oral Solid Dosage (OSD) manufacturing facility in Surendranagar, Gujarat.

Scheduled for Saturday, November 15, 2025, the event will be held from 10:00 AM to 4:00 PM at the plant itself. This is a prime opportunity for experienced professionals and fresh ITI candidates in the pharmaceutical sector to join a leading global organization.

Contents
Interview Venue:Open Positions and Eligibility CriteriaHow to Apply?FAQ:

Interview Venue:

Emcure Pharmaceuticals Limited,

New Survey No.485, Village: Kadu, Ta. Lakhtar, Dist.Surendranagar, Gujarat.

Open Positions and Eligibility Criteria

The company is looking to hire for multiple roles in Production, Warehouse, Engineering, Quality Assurance, Quality Control, and EHS. The detailed breakdown is as follows:

1. Production & Packing (OSD)

Positions: Officer, Executive, Technician

Experience: 1 to 5 years

Qualifications: M.Pharm, B.Pharm, ITI, Diploma

Relevant Areas: Granulation, Coating, Primary & Secondary Packing.

2. Warehouse

Positions: QMS, Officer, Executive

Experience: 2 to 6 years

Qualifications: B.Pharm, B.Sc, M.Sc

Key Skills: Knowledge of SAP/ERP, inventory management, GMP, GDP, and regulatory compliance.

3. Engineering

Positions: Officer, Executive, Electrician

Experience: 3 to 5 years

Qualifications: B.Tech/BE, Diploma, ITI

Relevant Areas: Plant Maintenance, QMS, Instrumentation, Utility Electrician (Breakdown).

4. Quality Assurance (OSD)

Position: Officer

Experience: 1 to 3 years

Qualifications: B.Pharm, M.Pharm, M.Sc, B.Sc

Key Skills: IPQA (In-Process Quality Assurance).

5. Quality Control & QC-Micro

Positions: Officer, Executive

Experience: 2 to 7 years

Qualifications: B.Sc, M.Sc, B.Pharm, M.Pharm

Key Skills: HPLC, LIMS, RM/PM/GLP, Analyst, AMV, MLT Testing, Environment Monitoring.

6. EHS (Environment, Health & Safety)

Position: Officer

Experience: 2 to 3 years

Qualifications: PDIS, B.Sc, M.Sc

Key Skills: ETP Operation, Environment Management, Fire Safety.

How to Apply?

Interested and eligible candidates are advised to attend the walk-in interview at the specified venue and time. Applicants must carry all relevant documents, including:

· Updated Resume

· Current CTC Proof (Salary Slip/Appointment Letter)

· Educational Certificates (All semesters/years)

· Experience Certificates

· Government ID Proof

For candidates who are unable to attend the interview in person, the company has provided an alternative application method. They can email their resumes to atish.patel@emcure.com.

The company has also specified that ITI freshers are welcome to attend the walk-in, indicating opportunities for entry-level positions as well.

This recruitment drive represents a valuable chance for skilled professionals to advance their careers with Emcure Pharmaceuticals, an organization dedicated to innovation, quality, and excellence in the healthcare sector.

Emcure Pharmaceuticals Walk-in Drive on November 15 2025
Emcure Pharmaceuticals Walk-in Drive on November 15 2025

FAQ:

1. What are the key steps involved in the Oral Solid Dosage (OSD) manufacturing process?

Answer:

The OSD manufacturing process typically includes the following steps:

Dispensing: Weighing and measuring raw materials as per the master formula record (MFR).

Granulation: Wet or dry granulation to achieve uniform particle size.

Drying: Moisture reduction using fluid bed dryers or tray dryers.

Compression: Tablet formation using rotary tablet presses.

Coating: Film or enteric coating for tablet protection and release control.

Packing: Primary (blister/strip) and secondary (carton) packing under controlled conditions.

Good understanding of GMP, BMR documentation, and in-process checks is essential.

2. What are common parameters checked during IPQA (In-Process Quality Assurance) in OSD manufacturing?

Answer:

IPQA ensures product quality at every stage. Key parameters include:

Granulation: LOD (Loss on Drying), particle size distribution.

Compression: Tablet weight variation, hardness, thickness, and disintegration time.

Coating: Appearance, weight gain, and uniformity.

Packing: Batch coding accuracy, sealing integrity, and label verification.

IPQA officers must also ensure line clearance, equipment cleanliness verification, and adherence to SOPs.

3. What are key tests performed in the Quality Control (QC) department for OSD products?

Answer:

QC testing involves multiple analytical and microbiological checks, such as:

Chemical Analysis: Assay, dissolution, uniformity of content, identification tests.

Instrumental Analysis: HPLC, GC, UV spectroscopy.

Raw Material (RM) and Packing Material (PM) Testing: As per pharmacopeial standards.

Microbiological Testing: Total viable count, MLT (Microbial Limit Test), environmental monitoring.

Stability Studies: Monitoring product quality under different storage conditions.

Proficiency in LIMS and GLP documentation is a major advantage.

4. What are the critical maintenance areas for an OSD plant’s engineering department?

Answer:

Engineering plays a vital role in plant reliability and compliance. Focus areas include:

Equipment Maintenance: Compression machines, coating pans, FBDs, blenders, HVAC systems.

Utility Systems: Boilers, water systems (RO, WFI), air compressors.

Instrumentation & Calibration: Ensuring all instruments meet required accuracy and are calibrated per schedule.

Electrical Maintenance: Panel boards, motors, and emergency power systems.

Documentation: Preventive maintenance records, calibration logs, and breakdown analysis reports.

Knowledge of QMS, BMR support, and GMP compliance is mandatory.

5. What are the major EHS (Environment, Health & Safety) protocols followed in a pharmaceutical plant?

Answer:

Key EHS protocols include:

Environment Management: Operation and monitoring of ETP/STP, waste segregation, and emission control.

Safety Procedures: Regular fire drills, use of PPE, hazard communication (MSDS), and risk assessments.

Health Protocols: Periodic medical check-ups, ergonomic practices, and safe material handling.

Incident Management: Immediate reporting, investigation, and corrective action for near-misses or accidents.

Compliance: Adherence to statutory norms (GPCB, Factories Act, etc.).

Candidates should be familiar with PDIS concepts, emergency response plans, and EHS audits.

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